A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1074256



Internal ID15580756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:145383210..145385252hg38UCSC Ensembl
Innerchr6:145704346..145706388hg19UCSC Ensembl
Innerchr6:145746039..145748081hg18UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg382043
hg192043
hg182043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604826
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)nssv1074256
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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