A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032695



Internal ID19121917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:9964852..10091632hg38UCSC Ensembl
Innerchr7:10004479..10131259hg19UCSC Ensembl
Innerchr7:9971004..10097784hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38126781
hg19126781
hg18126781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3752881
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)nsv1032695
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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