A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970185



Internal ID18605409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160491148..160491753hg38UCSC Ensembl
Innerchr6:160912180..160912785hg19UCSC Ensembl
Innerchr6:160832170..160832775hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38606
hg19606
hg18606
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2428977, nssv2428984, nssv2428980, nssv2428983, nssv2428978, nssv2428975, nssv2428976, nssv2428981, nssv2428979, nssv2428982
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)nsv970185
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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