A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18064069



Internal ID20631109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:75882632..75924160hg38UCSC Ensembl
chr1:76348317..76389845hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3841529
hg1941529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317788
Supporting Variants
Samples
Known GenesASB17, MSH4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18064069
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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