A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972767



Internal ID18261297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:83907740..83915531hg38UCSC Ensembl
Innerchr9:86522655..86530446hg19UCSC Ensembl
Innerchr9:85712475..85720266hg18UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg387792
hg197792
hg187792
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2555612, nssv2555606, nssv2555608, nssv2555610, nssv2555611, nssv2555614, nssv2555607, nssv2555615, nssv2555609, nssv2555613
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesKIF27
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972767
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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