A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984148



Internal ID18272652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84205093..84206783hg38UCSC Ensembl
Innerchr15:84873845..84875535hg19UCSC Ensembl
Innerchr15:82664849..82666539hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg381691
hg191691
hg181691
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2626813, nssv2626817, nssv2626811, nssv2626814, nssv2626818, nssv2626810, nssv2626812, nssv2626815, nssv2626816, nssv2626819
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesLOC388152, LOC440300
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv984148
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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