A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329789



Internal ID20862942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:211687072..211694137hg38UCSC Ensembl
chr1:211860414..211867479hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg387066
hg197066
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057436
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329789
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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