A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1765634



Internal ID17522998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:26474718..26476233hg38UCSC Ensembl
Innerchr1:26801209..26802724hg19UCSC Ensembl
Innerchr1:26673796..26675311hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381516
hg191516
hg181516
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv945842
Supporting Variants
SamplesHGDP01284
Known GenesHMGN2
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)nssv1765634
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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