A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18145751



Internal ID20712791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:55180492..55184314hg38UCSC Ensembl
chr6:55045290..55049112hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg383823
hg193823
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414346
Supporting Variants
Samples
Known GenesHCRTR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18145751
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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