A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1035176



Internal ID15888362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:78648334..78648895hg38UCSC Ensembl
Innerchr5:77944157..77944718hg19UCSC Ensembl
Innerchr5:77979913..77980474hg18UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38562
hg19562
hg18562
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598708
Supporting Variants
Samples
Known GenesLHFPL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1035176
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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