A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370269



Internal ID21027822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:159354716..159359868hg38UCSC Ensembl
chr3:159072505..159077657hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg385153
hg195153
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210383
Samples
Known GenesIQCJ-SCHIP1, SCHIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370269
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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