A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16907885



Internal ID6042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108731675..108731726hg38UCSC Ensembl
chr1:109274297..109274348hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5547039
Supporting Variants
Samples
Known GenesFNDC7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16907885
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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