A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023682



Internal ID19112899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89696294..89920681hg38UCSC Ensembl
Innerchr7:89325608..89549995hg19UCSC Ensembl
Innerchr7:89163544..89387931hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38224388
hg19224388
hg18224388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6528n100
Supporting Variantsnssv3755431
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)nsv1023682
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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