A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1755786



Internal ID17464222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16849164..16955509hg38UCSC Ensembl
Innerchr1:17175659..17282004hg19UCSC Ensembl
Innerchr1:17047977..17154591hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38106346
hg19106346
hg18106615
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv945800
Supporting Variants
SamplesHGDP00927
Known GenesCROCC, MIR3675
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)nssv1755786
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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