A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15197481



Internal ID21336277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61907877..61908031hg38UCSC Ensembl
chr5:61203704..61203858hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3951407
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15197481
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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