A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734131



Internal ID20510065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56776943..56777283hg38UCSC Ensembl
chr1:57242616..57242956hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260697
Samples
Known GenesC1orf168
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734131
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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