A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022646



Internal ID19111864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:9188210..9250078hg38UCSC Ensembl
Innerchr7:9227840..9289708hg19UCSC Ensembl
Innerchr7:9194365..9256233hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3861869
hg1961869
hg1861869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3642892
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)nsv1022646
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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