A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907303



Internal ID22682509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3227211..3227788hg38UCSC Ensembl
chr4:3228938..3229515hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38578
hg19578
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419873
Samples
Known GenesHTT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907303
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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