A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409501



Internal ID21067054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1893241..1895598hg38UCSC Ensembl
chr6:1893475..1895832hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg382358
hg192358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143101
Samples
Known GenesGMDS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409501
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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