A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350059



Internal ID21007612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:179959244..179959975hg38UCSC Ensembl
chr2:180823971..180824702hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg38732
hg19732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080910
Samples
Known GenesCWC22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350059
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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