A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17626807



Internal ID21818854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1701148..1709116hg38UCSC Ensembl
chr17:1604442..1612410hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg387969
hg197969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028335
Supporting Variants
Samples
Known GenesTLCD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17626807
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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