A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432597



Internal ID21394599
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 StatusM
Merged Variants
Supporting Variantsnssv15753973
SamplesNB08
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432597
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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