A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340096



Internal ID20997649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161924861..161937836hg38UCSC Ensembl
chr2:162781371..162794346hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg3812976
hg1912976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080155
Samples
Known GenesSLC4A10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340096
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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