A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606895



Internal ID16394304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:48783558..48855734hg38UCSC Ensembl
Innerchr7:48823154..48895330hg19UCSC Ensembl
Innerchr7:48793700..48865876hg18UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3872177
hg1972177
hg1872177
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154933
SamplesHGDP01311
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606895
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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