A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603164



Internal ID16043887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:55766964..55809540hg38UCSC Ensembl
Innerchr6:55631762..55674338hg19UCSC Ensembl
Innerchr6:55739721..55782297hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3842577
hg1942577
hg1842577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1060840
Samples
Known GenesBMP5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603164
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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