A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350841



Internal ID21008394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:115325301..115328300hg38UCSC Ensembl
chr2:116082877..116085876hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075693
Samples
Known GenesDPP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350841
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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