A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340879



Internal ID20998432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:186703801..186704600hg38UCSC Ensembl
chr2:187568528..187569327hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080695
Samples
Known GenesFAM171B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340879
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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