A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406871



Internal ID21064424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87596328..87615282hg38UCSC Ensembl
chr6:88306046..88325000hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3818955
hg1918955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149104
Samples
Known GenesORC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406871
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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