A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603638



Internal ID16044361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:69948540..70030414hg38UCSC Ensembl
Innerchr6:70658432..70740306hg19UCSC Ensembl
Innerchr6:70715153..70797027hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3881875
hg1981875
hg1881875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10758n54
Supporting Variantsnssv1063663
Samples
Known GenesCOL19A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603638
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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