A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2736227



Internal ID17760468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42665222..42670963hg38UCSC Ensembl
Innerchr9:44342025..44347766hg19UCSC Ensembl
Innerchr9:44282021..44287762hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg385742
hg195742
hg185742
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv969602
Supporting Variants
SamplesHGDP00542
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2736227
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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