A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980174



Internal ID18268688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:59101..59601hg38UCSC Ensembl
Innerchr4:58994..59494hg19UCSC Ensembl
Innerchr4:48994..49494hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2308886, nssv2308879, nssv2308880, nssv2308882, nssv2308885, nssv2308884, nssv2308883, nssv2308888, nssv2308887, nssv2308881
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesZNF595, ZNF718
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv980174
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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