A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037442



Internal ID20604482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67967701..67968500hg38UCSC Ensembl
chr17:65963817..65964616hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6532052
Supporting Variants
Samples
Known GenesBPTF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037442
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00655


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