A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066508



Internal ID19155727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:15500459..15922838hg38UCSC Ensembl
Innerchr22:16055171..16477504hg19UCSC Ensembl
Innerchr22:14435171..14857504hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38422380
hg19422334
hg18422334
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4451n100
Supporting Variantsnssv3589190, nssv3589179, nssv3731762, nssv3589199, nssv3589169, nssv3731760, nssv3589196, nssv3589187, nssv3589166, nssv3589189, nssv3731752, nssv3589184, nssv3731763, nssv3589193, nssv3589180, nssv3589172, nssv3589181, nssv3589197, nssv3589168, nssv3589167, nssv3589171, nssv3731749, nssv3589185, nssv3731761, nssv3589192, nssv3731764, nssv3589177, nssv3589198, nssv3731753, nssv3589178, nssv3731754, nssv3731751, nssv3589176, nssv3589200, nssv3589174, nssv3589186, nssv3589175, nssv3731758, nssv3731757, nssv3589182, nssv3589170, nssv3731756, nssv3589173, nssv3589191, nssv3731755, nssv3731765, nssv3731750, nssv3589194, nssv3589165, nssv3589195, nssv3589188, nssv3731759, nssv3589183
Samples
Known GenesBMS1P17, BMS1P18, OR11H1, POTEH
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066508
Frequency
Sample Size11257
Observed Gain51
Observed Loss2
Observed Complex0
Frequencyn/a


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