A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3504699



Internal ID18456294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46196488..46333389hg38UCSC Ensembl
Innerchr10:47567724..47704625hg19UCSC Ensembl
Innerchr10:47037730..47174631hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38136902
hg19136902
hg18136902
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037103
Supporting Variants
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3504699
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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