A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497089



Internal ID22555023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:64232346..64305398hg38UCSC Ensembl
chr4:65098064..65171116hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3873053
hg1973053
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839751
Supporting Variants
Samples
Known GenesTECRL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497089
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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