A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18015532



Internal ID20582572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:93546196..93592723hg38UCSC Ensembl
chr13:94198449..94244976hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3846528
hg1946528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6486581
Supporting Variants
Samples
Known GenesGPC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18015532
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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