A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033991



Internal ID18776525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38277957..38312264hg38UCSC Ensembl
Innerchr7:38317558..38351865hg19UCSC Ensembl
Innerchr7:38284083..38318390hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3834308
hg1934308
hg1834308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6329n100
Supporting Variantsnssv3643466
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033991
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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