A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735329



Internal ID20511271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:159748977..159749078hg38UCSC Ensembl
chr4:160670129..160670230hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263846
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735329
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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