A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031328



Internal ID19120550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:84553040..84748277hg38UCSC Ensembl
Innerchr7:84182356..84377593hg19UCSC Ensembl
Innerchr7:84020292..84215529hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38195238
hg19195238
hg18195238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6520n100
Supporting Variantsnssv3655165
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)nsv1031328
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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