A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433034



Internal ID21395036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:212198647..212199399hg38UCSC Ensembl
chr1:212371989..212372741hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg38753
hg19753
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15750975
SamplesMDQ045
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433034
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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