A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153053



Internal ID15879587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:97669437..97772855hg38UCSC Ensembl
Innerchr5:97005141..97108559hg19UCSC Ensembl
Innerchr5:97030897..97134315hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38103419
hg19103419
hg18103419
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598969
Supporting Variants
SamplesHGDP01399
Known GenesLOC102546227
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153053
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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