A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502346



Internal ID22560286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6239448..6240847hg38UCSC Ensembl
chr6:6239681..6241080hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845377
Supporting Variants
Samples
Known GenesF13A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502346
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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