A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015861



Internal ID19105079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62904802..63419173hg38UCSC Ensembl
Innerchr7:62365180..62879551hg19UCSC Ensembl
Innerchr7:62002615..62516986hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38514372
hg19514372
hg18514372
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6431n100
Supporting Variantsnssv3661956
Samples
Known GenesLOC100287704, LOC100287834, ZNF733P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015861
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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