A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2727285



Internal ID17878393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:60838702..60839496hg38UCSC Ensembl
Innerchr9:41424974..41425768hg19UCSC Ensembl
Innerchr9:41414974..41415768hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38795
hg19795
hg18795
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv973576
Supporting Variants
SamplesHGDP01307
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2727285
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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