A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331119



Internal ID20864280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26702016..26705651hg38UCSC Ensembl
chr1:27028507..27032142hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg383636
hg193636
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060609
Samples
Known GenesARID1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331119
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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