A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17496446



Internal ID22554380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:61764510..61769792hg38UCSC Ensembl
chr4:62630228..62635510hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg385283
hg195283
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839991
Supporting Variants
Samples
Known GenesLPHN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17496446
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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