A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607744



Internal ID16048467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88695106..90253815hg38UCSC Ensembl
Innerchr7:88324420..89883129hg19UCSC Ensembl
Innerchr7:88162356..89721065hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg381558710
hg191558710
hg181558710
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11493n54
Supporting Variantsnssv1155356
Samples1780854574_A
Known GenesC7orf62, C7orf63, DPY19L2P4, STEAP1, STEAP2, ZNF804B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607744
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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