A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712648



Internal ID136314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32357195..32357232hg38UCSC Ensembl
chr17:30684214..30684251hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5547568
Supporting Variants
Samples
Known GenesZNF207
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712648
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.006088


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