A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1070561



Internal ID15923747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:100547172..100637070hg38UCSC Ensembl
Innerchr6:100995048..101084946hg19UCSC Ensembl
Innerchr6:101101769..101191667hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3889899
hg1989899
hg1889899
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604264
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)nssv1070561
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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