A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526325



Internal ID15106932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56229817..56340666hg38UCSC Ensembl
Innerchr19:56741186..56852035hg19UCSC Ensembl
Innerchr19:61432998..61543847hg18UCSC Ensembl
Innerchr19:61432998..61543847hg17UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38110850
hg19110850
hg18110850
hg17110850
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702614
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526325
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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