A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523277



Internal ID15450570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15023114..15026431hg38UCSC Ensembl
Innerchr19:15133926..15137243hg19UCSC Ensembl
Innerchr19:14994926..14998243hg18UCSC Ensembl
Innerchr19:14994926..14998243hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg383318
hg193318
hg183318
hg173318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699011
Samples
Known GenesCCDC105
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523277
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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