A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3512323



Internal ID18810604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:55227709..55461237hg38UCSC Ensembl
Innerchr10:56987469..57220997hg19UCSC Ensembl
Innerchr10:56657475..56891003hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38233529
hg19233529
hg18233529
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049867
Supporting Variants
Samples
Known GenesRNU6-59P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3512323
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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