A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337141



Internal ID20994694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238537501..238540800hg38UCSC Ensembl
chr2:239446142..239449441hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084443
Samples
Known GenesLINC01107
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337141
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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