A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384504



Internal ID21042057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:149245381..149252768hg38UCSC Ensembl
chr4:150166533..150173920hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg387388
hg197388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112150
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384504
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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