A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317136



Internal ID20850220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:12530709..12532044hg38UCSC Ensembl
chr1:12590751..12592084hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381336
hg191334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051405
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317136
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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