A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545999



Internal ID15986722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:36394151..36401762hg38UCSC Ensembl
Innerchr1:36859752..36867363hg19UCSC Ensembl
Innerchr1:36632339..36639950hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg387612
hg197612
hg187612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv712328
Samples
Known GenesLSM10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545999
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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