A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373652



Internal ID21031205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7047549..7048272hg38UCSC Ensembl
chr4:7049276..7049999hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38724
hg19724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119119
Samples
Known GenesTADA2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373652
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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