A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029098



Internal ID18771630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12314482..12403416hg38UCSC Ensembl
Innerchr7:12354108..12443042hg19UCSC Ensembl
Innerchr7:12320633..12409567hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3888935
hg1988935
hg1888935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6272n100
Supporting Variantsnssv3642967
Samples
Known GenesVWDE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029098
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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