A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17490318



Internal ID22548240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156335093..156405387hg38UCSC Ensembl
chr4:157256245..157326539hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3870295
hg1970295
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5838366
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17490318
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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