A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351924



Internal ID21009477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:177323227..177328872hg38UCSC Ensembl
chr2:178187955..178193600hg19UCSC Ensembl
Cytoband2q31.2
Allele length
AssemblyAllele length
hg385646
hg195646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082107
Samples
Known GenesLOC100130691
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351924
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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