A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974562



Internal ID18609773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:40125026..40135151hg38UCSC Ensembl
Innerchr15:40417227..40427352hg19UCSC Ensembl
Innerchr15:38204519..38214644hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3810126
hg1910126
hg1810126
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2019061, nssv2019065, nssv2019070, nssv2019064, nssv2019069, nssv2019066, nssv2019067, nssv2019062, nssv2019063, nssv2019068
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974562
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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