A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404189



Internal ID21061742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2066309..2075392hg38UCSC Ensembl
chr6:2066543..2075626hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg389084
hg199084
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143212
Samples
Known GenesGMDS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404189
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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