A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945793



Internal ID18592643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16484768..16637149hg38UCSC Ensembl
Innerchr1:16811263..16963644hg19UCSC Ensembl
Innerchr1:16683850..16836231hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38152382
hg19152382
hg18152382
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1756350, nssv1756345, nssv1756352, nssv1756351, nssv1756344, nssv1756347, nssv1756348, nssv1756349, nssv1756346, nssv1756343
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCROCCP2, CROCCP3, MIR3675, NBPF1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945793
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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