A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350672



Internal ID21008225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:176992765..177014788hg38UCSC Ensembl
chr2:177857493..177879516hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3822024
hg1922024
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082090
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350672
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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