A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604916



Internal ID16392325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:153456411..153489668hg38UCSC Ensembl
Innerchr6:153777546..153810803hg19UCSC Ensembl
Innerchr6:153819239..153852496hg18UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3833258
hg1933258
hg1833258
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155098, nssv1155097
SamplesHGDP01238, HGDP01237
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604916
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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