A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1075206



Internal ID15928392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160843572..160858507hg38UCSC Ensembl
Innerchr6:161264604..161279539hg19UCSC Ensembl
Innerchr6:161184594..161199529hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3814936
hg1914936
hg1814936
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605022
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1075206
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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