A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340230



Internal ID20997783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9841294..9882350hg38UCSC Ensembl
chr2:9981423..10022479hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3841057
hg1941057
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18091699
Samples
Known GenesTAF1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340230
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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