A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012741



Internal ID19101958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89896137..90082510hg38UCSC Ensembl
Innerchr2:89934947..90121352hg19UCSC Ensembl
Innerchr2:89571989..89758657hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38186374
hg19186406
hg18186669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3973n100
Supporting Variantsnssv3579797, nssv3579798, nssv3579806, nssv3579803, nssv3579802, nssv3579799, nssv3579800, nssv3579801, nssv3579805, nssv3579804, nssv3579807
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)nsv1012741
Frequency
Sample Size11257
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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