A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3517534



Internal ID18469129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15828319..15902138hg38UCSC Ensembl
Innerchr10:15870318..15944137hg19UCSC Ensembl
Innerchr10:15910324..15984143hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3873820
hg1973820
hg1873820
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045879
Supporting Variants
Samples
Known GenesFAM188A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3517534
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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