A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1024211



Internal ID16318167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:9902228..9932098hg38UCSC Ensembl
Innerchr5:9902340..9932210hg19UCSC Ensembl
Innerchr5:9955340..9985210hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3829871
hg1929871
hg1829871
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597096
Supporting Variants
Samples
Known GenesLOC285692
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1024211
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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