A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545099



Internal ID15985822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:3077074..3139312hg38UCSC Ensembl
Innerchr1:2993638..3055876hg19UCSC Ensembl
Innerchr1:2983498..3045736hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3862239
hg1962239
hg1862239
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1172587
Samples1780862275_A
Known GenesMIR4251, PRDM16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545099
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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