A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372399



Internal ID21029952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157040004..157046437hg38UCSC Ensembl
chr3:156757793..156764226hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg386434
hg196434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096519
Samples
Known GenesLEKR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372399
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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