A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17466242



Internal ID22524132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13989019..13994418hg38UCSC Ensembl
chr10:14031019..14036418hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860716
Supporting Variants
Samples
Known GenesFRMD4A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17466242
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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