A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434607



Internal ID21396609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2144887..2146886hg38UCSC Ensembl
chr5:2145001..2147000hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15753531, nssv15753887, nssv15751382, nssv15749285, nssv15753190, nssv15745924, nssv15747447
SamplesNB12, SMI034, BTQ038, NB10, BTQ016, NB07, NB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434607
Frequency
Sample Size15
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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