A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326096



Internal ID20859230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209707189..209707604hg38UCSC Ensembl
chr1:209880534..209880949hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38416
hg19416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057268
Samples
Known GenesHSD11B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326096
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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