A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153696



Internal ID15531592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:43002769..43110718hg38UCSC Ensembl
Innerchr6:42970507..43078456hg19UCSC Ensembl
Innerchr6:43078485..43186434hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38107950
hg19107950
hg18107950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602994
Supporting Variants
SamplesHGDP01172
Known GenesCUL7, KLC4, KLHDC3, MEA1, MRPL2, PPP2R5D, PTK7, RRP36
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153696
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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