A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361138



Internal ID21018691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153472285..153477416hg38UCSC Ensembl
chr3:153190074..153195205hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg385132
hg195132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096064
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361138
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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