A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434872



Internal ID21396874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170266797..170267735hg38UCSC Ensembl
chr6:170575885..170576823hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38939
hg19939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv740n172
Supporting Variantsnssv15750804
SamplesNB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434872
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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