A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16999004



Internal ID66907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87163180..87163187hg38UCSC Ensembl
chr7:86792496..86792503hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5540309
Supporting Variants
Samples
Known GenesDMTF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16999004
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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