A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976960



Internal ID18265480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84117231..84429774hg38UCSC Ensembl
Innerchr15:84785983..84984473hg19UCSC Ensembl
Innerchr15:82576987..82775675hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38312544
hg19198491
hg18198689
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2035240, nssv2035241, nssv2035237, nssv2035235, nssv2035233, nssv2035239, nssv2035234, nssv2035232, nssv2035238, nssv2035236
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesDNM1P41, EFTUD1P1, GOLGA6L4, LOC100505679, LOC388152, LOC440300, LOC642423
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976960
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer