A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337770



Internal ID20995323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:186699803..186700285hg38UCSC Ensembl
chr2:187564530..187565012hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38483
hg19483
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080694
Samples
Known GenesFAM171B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337770
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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