A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740518



Internal ID20516494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6185340..6185429hg38UCSC Ensembl
chr6:6185573..6185662hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275331
Samples
Known GenesF13A1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740518
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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