A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351302



Internal ID21008855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:176658102..176658406hg38UCSC Ensembl
chr2:177522830..177523134hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082065
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351302
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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