A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837262



Internal ID22612197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102035700..102106235hg38UCSC Ensembl
chr4:102956857..103027392hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3870536
hg1970536
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497572, nssv17497571
Samples
Known GenesBANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837262
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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