A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028221



Internal ID19117439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:122178920..122259108hg38UCSC Ensembl
Innerchr7:121818974..121899162hg19UCSC Ensembl
Innerchr7:121606210..121686398hg18UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3880189
hg1980189
hg1880189
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6603n100
Supporting Variantsnssv3662121
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)nsv1028221
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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