A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322968



Internal ID20856083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8768823..8775963hg38UCSC Ensembl
chr1:8828882..8836022hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg387141
hg197141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064523
Samples
Known GenesRERE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322968
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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