A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007695



Internal ID19096914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:122922250..123005638hg38UCSC Ensembl
Innerchr2:123679826..123763214hg19UCSC Ensembl
Innerchr2:123396296..123479684hg18UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3883389
hg1983389
hg1883389
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4061n100
Supporting Variantsnssv3580703
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007695
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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