A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15748292



Internal ID21384590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8656010..8656503hg38UCSC Ensembl
chr17:8559328..8559821hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38494
hg19494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432640
Supporting Variants
SamplesBTQ016
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15748292
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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