A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317867



Internal ID20850957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36423740..36425517hg38UCSC Ensembl
chr1:36889341..36891118hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381778
hg191778
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061156
Samples
Known GenesOSCP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317867
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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