A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545824



Internal ID16333233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:24660386..24713376hg38UCSC Ensembl
Innerchr1:24986877..25039867hg19UCSC Ensembl
Innerchr1:24859464..24912454hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3852991
hg1952991
hg1852991
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173800
SamplesHGDP00974
Known GenesSRRM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545824
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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