A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612577



Internal ID16053300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:141326581..141448932hg38UCSC Ensembl
Innerchr8:142336680..142459032hg19UCSC Ensembl
Innerchr8:142405862..142528214hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38122352
hg19122353
hg18122353
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156892
SamplesHGDP00402
Known GenesGPR20, LOC731779, MROH5, PTP4A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612577
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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