A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434817



Internal ID21396819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165708842..165709639hg38UCSC Ensembl
chr6:166122330..166123127hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38798
hg19798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15751427
SamplesNB11
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434817
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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