A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050608



Internal ID19139827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:31822640..31861166hg38UCSC Ensembl
Innerchr10:32111568..32150094hg19UCSC Ensembl
Innerchr10:32151574..32190100hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3838527
hg1938527
hg1838527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3521069
Samples
Known GenesARHGAP12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050608
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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