A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3517193



Internal ID18468788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:124568787..124618034hg38UCSC Ensembl
Innerchr10:126257356..126306603hg19UCSC Ensembl
Innerchr10:126247346..126296593hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3849248
hg1949248
hg1849248
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050670
Supporting Variants
Samples
Known GenesLHPP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3517193
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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