A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1766477



Internal ID17737172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:27164334..27211307hg38UCSC Ensembl
Innerchr1:27490825..27537798hg19UCSC Ensembl
Innerchr1:27363412..27410385hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3846974
hg1946974
hg1846974
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv945846
Supporting Variants
SamplesHGDP00456
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)nssv1766477
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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