A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997910



Internal ID19157446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:52186336..52356952hg38UCSC Ensembl
Innerchr2:52413474..52584090hg19UCSC Ensembl
Innerchr2:52266978..52437594hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38170617
hg19170617
hg18170617
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3817n100
Supporting Variantsnssv3581706, nssv3581701, nssv3581704, nssv3581700, nssv3581707, nssv3581703, nssv3581708, nssv3581705, nssv3581702
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)nsv997910
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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