A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432801



Internal ID21090354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11724029..11725458hg38UCSC Ensembl
chr8:11581538..11582967hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg381430
hg191430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18163757
Samples
Known GenesGATA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432801
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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