A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024675



Internal ID19113892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:5828930..5925810hg38UCSC Ensembl
Innerchr7:5868561..5965441hg19UCSC Ensembl
Innerchr7:5835087..5931967hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3896881
hg1996881
hg1896881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6243n100
Supporting Variantsnssv3752804
Samples
Known GenesCCZ1, OCM, ZNF815P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024675
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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