A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016221



Internal ID19105440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:84553826..84748277hg38UCSC Ensembl
Innerchr7:84183142..84377593hg19UCSC Ensembl
Innerchr7:84021078..84215529hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38194452
hg19194452
hg18194452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6520n100
Supporting Variantsnssv3655166
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)nsv1016221
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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