A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371261



Internal ID21028814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13776387..13790377hg38UCSC Ensembl
chr3:13817884..13831874hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3813991
hg1913991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093862
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371261
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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