A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1766087



Internal ID17828441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:24672310..24673077hg38UCSC Ensembl
Innerchr1:24998801..24999568hg19UCSC Ensembl
Innerchr1:24871388..24872155hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38768
hg19768
hg18768
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv945828
Supporting Variants
SamplesHGDP00998
Known GenesSRRM1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1766087
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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