A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265509



Internal ID20474727
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 StatusS
Merged Variantsnsv4743377
Supporting Variants
Samples
Known GenesH6PD
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265509
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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