A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371241



Internal ID21028794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13720681..13849422hg38UCSC Ensembl
chr3:13762179..13890919hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38128742
hg19128741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095626
Samples
Known GenesLINC00620, WNT7A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371241
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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