A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2727447



Internal ID17871033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39821175..39825473hg38UCSC Ensembl
Innerchr9:41966193..41970491hg19UCSC Ensembl
Innerchr9:41956193..41960491hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg384299
hg194299
hg184299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982392
Supporting Variants
SamplesHGDP01284
Known GenesKGFLP2
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2727447
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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