A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17483060



Internal ID22540967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:97671993..97673521hg38UCSC Ensembl
chr2:98288456..98289984hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg381529
hg191529
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834161
Supporting Variants
Samples
Known GenesLINC01125
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17483060
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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