A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947929



Internal ID18248089
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 Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1844733, nssv1844731, nssv1844734, nssv1844732, nssv1844729, nssv1844727, nssv1844730, nssv1844735, nssv1844726, nssv1844728
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesGPRIN2, LINC00842, LOC100996758, NPY4R
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947929
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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