A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17500097



Internal ID22558033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104725175..104730878hg38UCSC Ensembl
chr7:104365622..104371325hg19UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg385704
hg195704
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854729
Supporting Variants
Samples
Known GenesLHFPL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17500097
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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