A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1842395



Internal ID17844410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38344519..38385618hg38UCSC Ensembl
Innerchr10:38633447..38674546hg19UCSC Ensembl
Innerchr10:38673453..38714552hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3841100
hg1941100
hg1841100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv947859
Supporting Variants
SamplesHGDP01029
Known GenesHSD17B7P2, SEPT7P9
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1842395
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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