A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545264



Internal ID15985987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:6457119..6492439hg38UCSC Ensembl
Innerchr1:6517179..6552499hg19UCSC Ensembl
Innerchr1:6439766..6475086hg18UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3835321
hg1935321
hg1835321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv709210
Samples
Known GenesESPN, PLEKHG5, TNFRSF25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545264
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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