A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346838



Internal ID21004391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:210106100..210107366hg38UCSC Ensembl
chr2:210970824..210972090hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg381267
hg191267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085111
Samples
Known GenesKANSL1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346838
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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