A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749991



Internal ID20526026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150743560..150743623hg38UCSC Ensembl
chr1:150716036..150716099hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266457
Samples
Known GenesCTSS
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749991
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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