A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17498642



Internal ID22556577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:96173709..96184460hg38UCSC Ensembl
chr4:97094860..97105611hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3810752
hg1910752
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839907
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17498642
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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