A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17498717



Internal ID22556652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76857935..76866043hg38UCSC Ensembl
chr5:76153760..76161868hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg388109
hg198109
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843491
Supporting Variants
Samples
Known GenesS100Z
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17498717
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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