A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3707759



Internal ID19006040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38407736..38780907hg38UCSC Ensembl
Innerchr10:38696664..39074038hg19UCSC Ensembl
Innerchr10:38736670..39114044hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38373172
hg19377375
hg18377375
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043781
Supporting Variants
Samples
Known GenesACTR3BP5, LINC00999
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3707759
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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