A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431142



Internal ID21393144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99460765..99462548hg38UCSC Ensembl
chr10:101220522..101222305hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg381784
hg191784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15752789, nssv15751392, nssv15747570, nssv15745988, nssv15746086
SamplesNB12, SMI034, MDQ010, NB11, MDQ025
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431142
Frequency
Sample Size15
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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