A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3515944



Internal ID18467539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132834544..132988338hg38UCSC Ensembl
Innerchr10:134648048..134801842hg19UCSC Ensembl
Innerchr10:134498038..134651832hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38153795
hg19153795
hg18153795
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049415
Supporting Variants
Samples
Known GenesLOC399829, TTC40
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3515944
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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