A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1844731



Internal ID17389954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46417726..46574536hg38UCSC Ensembl
Innerchr10:46975081..47132029hg19UCSC Ensembl
Innerchr10:46395087..46552035hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38156811
hg19156949
hg18156949
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsnsv947929
Supporting Variants
SamplesHGDP00456
Known GenesGPRIN2, LINC00842, LOC100996758, NPY4R
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1844731
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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