A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2607236



Internal ID17844645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38472039..38529907hg38UCSC Ensembl
Innerchr10:38760967..38818835hg19UCSC Ensembl
Innerchr10:38800973..38859132hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3857869
hg1957869
hg1858160
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948264
Supporting Variants
SamplesHGDP01029
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2607236
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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