A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017124



Internal ID19106341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:84542150..84689668hg38UCSC Ensembl
Innerchr7:84171466..84318984hg19UCSC Ensembl
Innerchr7:84009402..84156920hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38147519
hg19147519
hg18147519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6519n100
Supporting Variantsnssv3655164
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)nsv1017124
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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