A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1074253



Internal ID15927439
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 StatusS
Merged Variantsnsv604822
Supporting Variants
Samples
Known GenesUTRN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1074253
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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