A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037533



Internal ID20604573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7544661..7546281hg38UCSC Ensembl
chr17:7447978..7449598hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381621
hg191621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513173
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037533
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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