A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3512096



Internal ID18810377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:124231721..124308922hg38UCSC Ensembl
Innerchr10:125920290..125997491hg19UCSC Ensembl
Innerchr10:125910280..125987481hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3877202
hg1977202
hg1877202
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049635
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3512096
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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