A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965781



Internal ID18254325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160467442..160478795hg38UCSC Ensembl
Innerchr6:160888474..160899827hg19UCSC Ensembl
Innerchr6:160808464..160819817hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3811354
hg1911354
hg1811354
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2430015, nssv2430010, nssv2430017, nssv2430012, nssv2430018, nssv2430014, nssv2430011, nssv2430019, nssv2430013, nssv2430016
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)nsv965781
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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