A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15753973



Internal ID21389017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75076670..75077516hg38UCSC Ensembl
chr17:73072765..73073611hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38847
hg19847
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432597
Supporting Variants
SamplesNB08
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15753973
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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