A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351601



Internal ID21009154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:118859070..118861501hg38UCSC Ensembl
chr2:119616646..119619077hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg382432
hg192432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075863
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351601
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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