A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17494929



Internal ID22552861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132309313..132319601hg38UCSC Ensembl
chr5:131645006..131655294hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3810289
hg1910289
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5841124
Supporting Variants
Samples
Known GenesLOC553103, SLC22A4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17494929
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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