A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4447623



Internal ID22113800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3227192..3227260hg38UCSC Ensembl
chr4:3228919..3228987hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761513
Samples
Known GenesHTT
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4447623
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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