A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598708



Internal ID16386117
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 StatusM
Merged Variants
Supporting Variantsnssv1035176, nssv1035175
Samples
Known GenesLHFPL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598708
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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