A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031583



Internal ID19120805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:5849380..5931291hg38UCSC Ensembl
Innerchr7:5889011..5970922hg19UCSC Ensembl
Innerchr7:5855537..5937448hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3881912
hg1981912
hg1881912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6243n100
Supporting Variantsnssv3752807
Samples
Known GenesCCZ1, OCM, RSPH10B, RSPH10B2, ZNF815P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031583
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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