A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1853064



Internal ID17762261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68631969..68634281hg38UCSC Ensembl
Innerchr10:70391726..70394038hg19UCSC Ensembl
Innerchr10:70061732..70064044hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg382313
hg192313
hg182313
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948048
Supporting Variants
SamplesHGDP00542
Known GenesTET1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1853064
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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