A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1049414



Internal ID15902600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:11509090..11581757hg38UCSC Ensembl
Innerchr6:11509323..11581990hg19UCSC Ensembl
Innerchr6:11617309..11689976hg18UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg3872668
hg1972668
hg1872668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600989
Supporting Variants
Samples
Known GenesTMEM170B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1049414
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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