A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173800



Internal ID15877360
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 StatusS
Merged Variantsnsv545824
Supporting Variants
SamplesHGDP00974
Known GenesSRRM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173800
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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