A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040229



Internal ID19129448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122380131..122432958hg38UCSC Ensembl
Innerchr10:124139647..124192474hg19UCSC Ensembl
Innerchr10:124129637..124182464hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3852828
hg1952828
hg1852828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv987n100
Supporting Variantsnssv3511873
Samples
Known GenesMIR3941, PLEKHA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040229
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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