A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17635800



Internal ID21827847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9600971..9601135hg38UCSC Ensembl
chr17:9504288..9504452hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027174
Supporting Variants
Samples
Known GenesWDR16
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17635800
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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