A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968604



Internal ID18603832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28145986..28150767hg38UCSC Ensembl
Innerchr9:28145984..28150765hg19UCSC Ensembl
Innerchr9:28135984..28140765hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg384782
hg194782
hg184782
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2525614, nssv2525620, nssv2525612, nssv2525617, nssv2722885, nssv2722886, nssv2722892, nssv2722893, nssv2525618, nssv2525613, nssv2722890, nssv2525611, nssv2722887, nssv2722884, nssv2525615, nssv2525616, nssv2722891, nssv2525619, nssv2722889, nssv2722888
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLINGO2
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968604
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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