A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352755



Internal ID21010308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:137030149..137142170hg38UCSC Ensembl
chr2:137787719..137899740hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg38112022
hg19112022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077986
Samples
Known GenesTHSD7B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352755
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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