A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730302



Internal ID20506213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:57150316..57150429hg38UCSC Ensembl
chr1:57615989..57616102hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290440
Samples
Known GenesDAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730302
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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