A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837764



Internal ID22612699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155181534..155187133hg38UCSC Ensembl
chr4:156102686..156108285hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499712
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837764
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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