A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352255



Internal ID21009808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:188353284..188600298hg38UCSC Ensembl
chr2:189218011..189465025hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38247015
hg19247015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082834
Samples
Known GenesGULP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352255
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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