A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434129



Internal ID21396131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:101039000..101040030hg38UCSC Ensembl
chr4:101960157..101961187hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg381031
hg191031
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15749664, nssv15754002, nssv15752721, nssv15749962, nssv15745817, nssv15749457, nssv15751986
SamplesNB08, BTQ038, BTQ055, SMI041, SMI018, MDQ025, NB09
Known GenesPPP3CA
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434129
Frequency
Sample Size15
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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