A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409427



Internal ID21066980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:74125601..74127200hg38UCSC Ensembl
chr6:74835317..74836916hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148143
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409427
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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