A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17493636



Internal ID22551565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:177045988..177129322hg38UCSC Ensembl
chr4:177967142..178050476hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3883335
hg1983335
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5838454
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17493636
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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