A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17491068



Internal ID22548993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82992820..82997625hg38UCSC Ensembl
chr4:83913973..83918778hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg384806
hg194806
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5840130
Supporting Variants
Samples
Known GenesLIN54
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17491068
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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