A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606813



Internal ID16394222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:44959115..44962092hg38UCSC Ensembl
Innerchr7:44998714..45001691hg19UCSC Ensembl
Innerchr7:44965239..44968216hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg382978
hg192978
hg182978
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11312n54
Supporting Variantsnssv1083564
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606813
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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