A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18013084



Internal ID20580124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:71015624..71016046hg38UCSC Ensembl
chr13:71589756..71590178hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6485623
Supporting Variants
Samples
Known GenesLINC00348
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18013084
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0009


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