A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341267



Internal ID20998820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231420917..231454846hg38UCSC Ensembl
chr2:232285628..232319557hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3833930
hg1933930
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086576
Samples
Known GenesNCL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341267
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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