A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327397



Internal ID20860535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209675001..209676100hg38UCSC Ensembl
chr1:209848346..209849445hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057267
Samples
Known GenesG0S2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327397
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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