A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052251



Internal ID20619291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156060273..156061498hg38UCSC Ensembl
chr1:156030064..156031289hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg381226
hg191226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324448
Supporting Variants
Samples
Known GenesMIR7851, RAB25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052251
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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