A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17003317



Internal ID69830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137300977..137300977hg38UCSC Ensembl
chr7:136985724..136985724hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38562
hg19562
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5547606
Supporting Variants
Samples
Known GenesPTN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17003317
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.007837


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