A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607013



Internal ID16394422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:53392993..53522557hg38UCSC Ensembl
Innerchr7:53460686..53590250hg19UCSC Ensembl
Innerchr7:53428180..53557744hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38129565
hg19129565
hg18129565
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11348n54
Supporting Variantsnssv1084630, nssv1084641, nssv1084635, nssv1084632, nssv1084631, nssv1084642, nssv1154943, nssv1154942, nssv1084637, nssv1084640, nssv1154946, nssv1084638, nssv1084633, nssv1154945, nssv1084636, nssv1154944, nssv1084639, nssv1084634
SamplesHGDP00041, HGDP00567, HGDP00098, HGDP00743, HGDP00338
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607013
Frequency
Sample Size17421
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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