A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963381



Internal ID18598622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:177623664..177624386hg38UCSC Ensembl
Innerchr3:177341452..177342174hg19UCSC Ensembl
Innerchr3:178824146..178824868hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38723
hg19723
hg18723
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2297971, nssv2297970, nssv2297969, nssv2297964, nssv2297967, nssv2297968, nssv2297965, nssv2297966, nssv2297972, nssv2297963
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLINC00578
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963381
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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