A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044664



Internal ID19133883
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 StatusM
Merged Variantsdgv998n100
Supporting Variantsnssv3516337
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)nsv1044664
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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