A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294187



Internal ID20503405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:61914523..61915643hg38UCSC Ensembl
chr17:59991884..59993004hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg381121
hg191121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744520
Supporting Variants
Samples
Known GenesINTS2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294187
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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