A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509098



Internal ID22567048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102926607..102928306hg38UCSC Ensembl
chr7:102567054..102568753hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862332
Supporting Variants
Samples
Known GenesFBXL13, LRRC17
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509098
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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