A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1049073



Internal ID15902259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:7775784..7782286hg38UCSC Ensembl
Innerchr6:7776017..7782519hg19UCSC Ensembl
Innerchr6:7721016..7727518hg18UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg386503
hg196503
hg186503
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600917
Supporting Variants
Samples
Known GenesBMP6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1049073
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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