A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970183



Internal ID18258721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160482499..160487694hg38UCSC Ensembl
Innerchr6:160903531..160908726hg19UCSC Ensembl
Innerchr6:160823521..160828716hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg385196
hg195196
hg185196
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2430116, nssv2430111, nssv2430113, nssv2430110, nssv2430109, nssv2430115, nssv2430114, nssv2430108, nssv2430107, nssv2430112
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLPAL2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970183
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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