A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141751



Internal ID20708791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36427201..36428900hg38UCSC Ensembl
chr6:36394978..36396677hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402197
Supporting Variants
Samples
Known GenesPXT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141751
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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