A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3706193



Internal ID18657788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:91075976..91154665hg38UCSC Ensembl
Innerchr10:92835733..92914422hg19UCSC Ensembl
Innerchr10:92825713..92904402hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3878690
hg1978690
hg1878690
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048584
Supporting Variants
Samples
Known GenesNUDT9P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3706193
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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