A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011600



Internal ID19100817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89896137..90209906hg38UCSC Ensembl
Innerchr2:89934947..90248772hg19UCSC Ensembl
Innerchr2:89571989..89886077hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38313770
hg19313826
hg18314089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3975n100
Supporting Variantsnssv3579820, nssv3579818, nssv3579822, nssv3579819, nssv3579821, nssv3579817
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)nsv1011600
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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