A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1064495



Internal ID15917681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:74122829..74126569hg38UCSC Ensembl
Innerchr6:74832545..74836285hg19UCSC Ensembl
Innerchr6:74889265..74893005hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg383741
hg193741
hg183741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603755
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)nssv1064495
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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