A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434975



Internal ID21396977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42869830..42871804hg38UCSC Ensembl
chr6:42837568..42839542hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381975
hg191975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv696n172
Supporting Variantsnssv15749297, nssv15748619
SamplesNB12, MDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434975
Frequency
Sample Size15
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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