A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419699



Internal ID21077252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10971219..10975903hg38UCSC Ensembl
chr8:10828729..10833413hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg384685
hg194685
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162894
Samples
Known GenesXKR6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419699
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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