A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019461



Internal ID18761996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62284144..63523932hg38UCSC Ensembl
Innerchr7:61728395..62984310hg19UCSC Ensembl
Innerchr7:61365830..62621745hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg381239789
hg191255916
hg181255916
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6397n100
Supporting Variantsnssv3752994
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)nsv1019461
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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