A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1053547



Internal ID15560047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31870664..31939370hg38UCSC Ensembl
Innerchr6:31838441..31907147hg19UCSC Ensembl
Innerchr6:31946420..32015126hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3868707
hg1968707
hg1868707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601960
Supporting Variants
Samples
Known GenesC2, EHMT2, LOC102060414, SLC44A4, ZBTB12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1053547
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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