A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431395



Internal ID21393397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8427327..8428306hg38UCSC Ensembl
chr10:8469290..8470269hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38980
hg19980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15749817, nssv15750550
SamplesSMI034, SMI041
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431395
Frequency
Sample Size15
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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