A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17481989



Internal ID22539894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202642497..202650675hg38UCSC Ensembl
chr2:203507220..203515398hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg388179
hg198179
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5832370
Supporting Variants
Samples
Known GenesFAM117B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17481989
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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