A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712649



Internal ID136315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32367280..32367316hg38UCSC Ensembl
chr17:30694299..30694335hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5545407
Supporting Variants
Samples
Known GenesZNF207
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712649
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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