A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2727487



Internal ID17812801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39862320..39877863hg38UCSC Ensembl
Innerchr9:42007338..42022881hg19UCSC Ensembl
Innerchr9:41997338..42012881hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3815544
hg1915544
hg1815544
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982394
Supporting Variants
SamplesHGDP00927
Known GenesKGFLP2, LOC643648
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2727487
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer