A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153530



Internal ID15879172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:16834459..16848091hg38UCSC Ensembl
Innerchr5:16834568..16848200hg19UCSC Ensembl
Innerchr5:16887568..16901200hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3813633
hg1913633
hg1813633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597310
Supporting Variants
SamplesHGDP01321
Known GenesMYO10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153530
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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