A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968738



Internal ID18603966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:99998544..100005759hg38UCSC Ensembl
Innerchr9:102760826..102768041hg19UCSC Ensembl
Innerchr9:101800647..101807862hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg387216
hg197216
hg187216
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2561429, nssv2561431, nssv2561426, nssv2561432, nssv2561433, nssv2561430, nssv2561427, nssv2561428, nssv2561425, nssv2561434
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesERP44
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968738
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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