A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1057872



Internal ID15564372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:34142480..34295966hg38UCSC Ensembl
Innerchr6:34110257..34263743hg19UCSC Ensembl
Innerchr6:34218235..34371721hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38153487
hg19153487
hg18153487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602863
Supporting Variants
Samples
Known GenesC6orf1, GRM4, HMGA1, MIR6835, NUDT3, RPS10-NUDT3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1057872
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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