A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977719



Internal ID18612925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58856010..58857101hg38UCSC Ensembl
Innerchr15:59148209..59149300hg19UCSC Ensembl
Innerchr15:56935501..56936592hg18UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg381092
hg191092
hg181092
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2026671, nssv2026665, nssv2026667, nssv2026672, nssv2026663, nssv2026670, nssv2026668, nssv2026669, nssv2026664, nssv2026666
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAM63B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977719
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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