A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350379



Internal ID21007932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:112913843..112914676hg38UCSC Ensembl
chr2:113671420..113672253hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38834
hg19834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075585
Samples
Known GenesIL37
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350379
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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