A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2730009



Internal ID17841772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65257657..65262060hg38UCSC Ensembl
Innerchr9:42740371..42744875hg19UCSC Ensembl
Innerchr9:42730367..42734871hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg384404
hg194505
hg184505
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982411
Supporting Variants
SamplesHGDP00998
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2730009
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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