A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973370



Internal ID18608585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65282353..65302240hg38UCSC Ensembl
Innerchr9:70175959..70195846hg19UCSC Ensembl
Innerchr9:69465779..69485666hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3819888
hg1919888
hg1819888
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2754343, nssv2754770, nssv2747583, nssv2752916, nssv2753980, nssv2750759, nssv2747894, nssv2753983, nssv2752912, nssv2746848
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFOXD4L5
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv973370
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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