A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320231



Internal ID20853329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:75898502..75913738hg38UCSC Ensembl
chr1:76364187..76379423hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3815237
hg1915237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064071
Samples
Known GenesMSH4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320231
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer