A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1035172



Internal ID15888358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:78648231..78648821hg38UCSC Ensembl
Innerchr5:77944054..77944644hg19UCSC Ensembl
Innerchr5:77979810..77980400hg18UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38591
hg19591
hg18591
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598705
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)nssv1035172
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer