A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17489123



Internal ID22547042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:97672411..97687865hg38UCSC Ensembl
chr2:98288874..98304328hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3815455
hg1915455
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834162
Supporting Variants
Samples
Known GenesLINC01125
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17489123
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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