A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604822



Internal ID16392231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:144647059..144680751hg38UCSC Ensembl
Innerchr6:144968195..145001887hg19UCSC Ensembl
Innerchr6:145009888..145043580hg18UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3833693
hg1933693
hg1833693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1074253
Samples
Known GenesUTRN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604822
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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