A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319911



Internal ID20853008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:75829700..75946482hg38UCSC Ensembl
chr1:76295385..76412167hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38116783
hg19116783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064062
Samples
Known GenesASB17, MSH4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319911
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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