A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317364



Internal ID20850448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93990818..93992074hg38UCSC Ensembl
chr1:94456374..94457630hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg381257
hg191257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065603
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317364
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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