A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156386



Internal ID15877805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:143904439..143985257hg38UCSC Ensembl
Innerchr8:144978607..145059425hg19UCSC Ensembl
Innerchr8:145050595..145131413hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3880819
hg1980819
hg1880819
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612901
Supporting Variants
SamplesHGDP01048
Known GenesMIR661, PARP10, PLEC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156386
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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