A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15746171



Internal ID21385741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:217909322..217909555hg38UCSC Ensembl
chr1:218082664..218082897hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433036
Supporting Variants
SamplesBTQ055
Known GenesLINC00210
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15746171
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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