A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17498666



Internal ID22556601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99149600..99151349hg38UCSC Ensembl
chr4:100070757..100072506hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg381750
hg191750
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5840236
Supporting Variants
Samples
Known GenesLOC100507053
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17498666
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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