A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551523



Internal ID15992246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73873999..73875375hg38UCSC Ensembl
Innerchr10:75633757..75635133hg19UCSC Ensembl
Innerchr10:75303763..75305139hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg381377
hg191377
hg181377
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv750282, nssv750281
Samples
Known GenesCAMK2G
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551523
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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