A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1755652



Internal ID17761389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15792862..15796022hg38UCSC Ensembl
Innerchr1:16119357..16122517hg19UCSC Ensembl
Innerchr1:15991944..15995104hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg383161
hg193161
hg183161
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv945788
Supporting Variants
SamplesHGDP00542
Known Genes
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)nssv1755652
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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