A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052265



Internal ID20619305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156371448..156379191hg38UCSC Ensembl
chr1:156341239..156348982hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg387744
hg197744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6333940
Supporting Variants
Samples
Known GenesRHBG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052265
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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