A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840714



Internal ID22615649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117956565..117963164hg38UCSC Ensembl
chr5:117292260..117298859hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg386600
hg196600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499972
Samples
Known GenesLOC102467224
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840714
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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