A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1064484



Internal ID15917670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:74122808..74142296hg38UCSC Ensembl
Innerchr6:74832524..74852012hg19UCSC Ensembl
Innerchr6:74889244..74908732hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3819489
hg1919489
hg1819489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603752
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1064484
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer