A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743377



Internal ID20519365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9250360..9250436hg38UCSC Ensembl
chr1:9310419..9310495hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265509
Samples
Known GenesH6PD
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743377
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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