A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3516337



Internal ID18814618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132998894..133170978hg38UCSC Ensembl
Innerchr10:134812398..134984482hg19UCSC Ensembl
Innerchr10:134662388..134834472hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38172085
hg19172085
hg18172085
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044664
Supporting Variants
Samples
Known GenesGPR123, KNDC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3516337
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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