A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975798



Internal ID18264319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46231739..46254652hg38UCSC Ensembl
Innerchr10:47602975..47625888hg19UCSC Ensembl
Innerchr10:47072981..47095894hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3822914
hg1922914
hg1822914
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2764830, nssv2761467, nssv2759811, nssv2756724, nssv2759961, nssv2759741, nssv2764667, nssv2762525, nssv2758140
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesANTXRLP1
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975798
Frequency
Sample Size10
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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