A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036414



Internal ID20603454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:52873915..53022120hg38UCSC Ensembl
chr17:50951275..51099480hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38148206
hg19148206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6525250
Supporting Variants
Samples
Known GenesC17orf112
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036414
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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