A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702424



Internal ID15439076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54600262..54611839hg38UCSC Ensembl
Innerchr19:55111727..55123305hg19UCSC Ensembl
Innerchr19:59803539..59815117hg18UCSC Ensembl
Innerchr19:59803539..59815117hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3811578
hg1911579
hg1811579
hg1711579
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516569
Supporting Variants
Samples
Known GenesLILRA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702424
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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