A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1070565



Internal ID15923751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:100611010..100748204hg38UCSC Ensembl
Innerchr6:101058886..101196080hg19UCSC Ensembl
Innerchr6:101165607..101302801hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38137195
hg19137195
hg18137195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604270
Supporting Variants
Samples
Known GenesASCC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1070565
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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