A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409977



Internal ID21067530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1404601..1410000hg38UCSC Ensembl
chr6:1404836..1410235hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138571
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409977
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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