A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024555



Internal ID18767087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:5816432..5890951hg38UCSC Ensembl
Innerchr7:5856063..5930582hg19UCSC Ensembl
Innerchr7:5822589..5897108hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3874520
hg1974520
hg1874520
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6242n100
Supporting Variantsnssv3655068
Samples
Known GenesOCM, ZNF815P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024555
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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