A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2754364



Internal ID17755335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65166952..65169800hg38UCSC Ensembl
Innerchr9:70060552..70063406hg19UCSC Ensembl
Innerchr9:69350372..69353226hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg382849
hg192855
hg182855
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972393
Supporting Variants
SamplesHGDP00521
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2754364
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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