A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv652344



Internal ID15388996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35169605..35171906hg38UCSC Ensembl
Innerchr19:35660508..35662809hg19UCSC Ensembl
Innerchr19:40352348..40354649hg18UCSC Ensembl
Innerchr19:40352348..40354649hg17UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg382302
hg192302
hg182302
hg172302
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516540
Supporting Variants
Samples
Known GenesFXYD5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv652344
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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