A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522620



Internal ID15103227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12486691..12491289hg38UCSC Ensembl
Innerchr10:12528690..12533288hg19UCSC Ensembl
Innerchr10:12568696..12573294hg18UCSC Ensembl
Innerchr10:12568696..12573294hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg384599
hg194599
hg184599
hg174599
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706016
Samples
Known GenesCAMK1D
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522620
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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