A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400166



Internal ID21057719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:8760401..8770400hg38UCSC Ensembl
chr6:8760634..8770633hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3810000
hg1910000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149105
Samples
Known GenesLOC100506207
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400166
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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