A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3731770



Internal ID19030051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:15533098..15896848hg38UCSC Ensembl
Innerchr22:16081115..16444865hg19UCSC Ensembl
Innerchr22:14461115..14824865hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38363751
hg19363751
hg18363751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057319
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, POTEH
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3731770
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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