A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17494339



Internal ID22552269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:19104824..19228755hg38UCSC Ensembl
chr4:19106447..19230378hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38123932
hg19123932
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839211
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17494339
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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