A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456319



Internal ID22514196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:152303277..152305337hg38UCSC Ensembl
chr1:152275753..152277813hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg382061
hg192061
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828356
Supporting Variants
Samples
Known GenesFLG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456319
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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