A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350182



Internal ID21007735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:114519985..114520567hg38UCSC Ensembl
chr2:115277562..115278144hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075248
Samples
Known GenesDPP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350182
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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