A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525329



Internal ID15105936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52833114..52889834hg38UCSC Ensembl
Innerchr19:53336367..53393087hg19UCSC Ensembl
Innerchr19:58028179..58084899hg18UCSC Ensembl
Innerchr19:58028179..58084899hg17UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3856721
hg1956721
hg1856721
hg1756721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701439
Samples
Known GenesZNF320, ZNF468
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525329
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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