A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525499



Internal ID15452792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7829846..7856737hg38UCSC Ensembl
Innerchr19:7894732..7921623hg19UCSC Ensembl
Innerchr19:7800732..7827623hg18UCSC Ensembl
Innerchr19:7800732..7827623hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3826892
hg1926892
hg1826892
hg1726892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701631
Samples
Known GenesEVI5L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525499
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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