A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2662146



Internal ID17850099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:15228131..15252227hg38UCSC Ensembl
Innerchr18:15228130..15252226hg19UCSC Ensembl
Innerchr18:15218130..15242226hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3824097
hg1924097
hg1824097
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv960681
Supporting Variants
SamplesHGDP01029
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2662146
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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