A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434176



Internal ID21396178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:127831522..127832088hg38UCSC Ensembl
chr4:128752677..128753243hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv586n172
Supporting Variantsnssv15747283
SamplesNB07
Known GenesHSPA4L
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434176
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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