A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033292



Internal ID19122514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62553935..63292311hg38UCSC Ensembl
Innerchr7:62014313..62752689hg19UCSC Ensembl
Innerchr7:61651748..62390124hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38738377
hg19738377
hg18738377
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6411n100
Supporting Variantsnssv3661835
Samples
Known GenesZNF733P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033292
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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