A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947748



Internal ID18247909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15154172..15157288hg38UCSC Ensembl
Innerchr10:15196171..15199287hg19UCSC Ensembl
Innerchr10:15236177..15239293hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg383117
hg193117
hg183117
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1832196, nssv1832194, nssv1832193, nssv1832201, nssv1832200, nssv1832195, nssv1832199, nssv1832202, nssv1832197, nssv1832198
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesNMT2, PPIAP30
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947748
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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