A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017260



Internal ID19106477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:83763785..83877327hg38UCSC Ensembl
Innerchr7:83393101..83506643hg19UCSC Ensembl
Innerchr7:83231037..83344579hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38113543
hg19113543
hg18113543
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6518n100
Supporting Variantsnssv3655159, nssv3655160
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)nsv1017260
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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