A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967814



Internal ID18603042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:173418296..173420823hg38UCSC Ensembl
Innerchr4:174339447..174341974hg19UCSC Ensembl
Innerchr4:174576022..174578549hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg382528
hg192528
hg182528
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2340992, nssv2340987, nssv2340995, nssv2340988, nssv2340990, nssv2340994, nssv2340993, nssv2340991, nssv2340986, nssv2340989
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967814
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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