A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525108



Internal ID15105715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35086966..35099016hg38UCSC Ensembl
Innerchr19:35577870..35589920hg19UCSC Ensembl
Innerchr19:40269710..40281760hg18UCSC Ensembl
Innerchr19:40269710..40281760hg17UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3812051
hg1912051
hg1812051
hg1712051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701168
Samples
Known GenesHPN-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525108
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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