A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434881



Internal ID21396883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:18401860..18402636hg38UCSC Ensembl
chr6:18402091..18402867hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38777
hg19777
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv679n172
Supporting Variantsnssv15751408, nssv15747696, nssv15754415, nssv15745723, nssv15746241, nssv15754616, nssv15752800, nssv15751904, nssv15749267, nssv15745942, nssv15752685, nssv15748312
SamplesSMI034, NB08, BTQ038, NB10, BTQ055, MDQ010, BTQ016, SMI041, NB07, SMI018, MDQ025, NB09
Known GenesRNF144B
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434881
Frequency
Sample Size15
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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