A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434974



Internal ID21396976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42869830..42871522hg38UCSC Ensembl
chr6:42837568..42839260hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381693
hg191693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv696n172
Supporting Variantsnssv15753943
SamplesBTQ055
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434974
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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