A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607790



Internal ID16395199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90537591..90592034hg38UCSC Ensembl
Innerchr7:90166905..90221348hg19UCSC Ensembl
Innerchr7:90004841..90059284hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3854444
hg1954444
hg1854444
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11498n54
Supporting Variantsnssv1155364
SamplesHGDP01198
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607790
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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