A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431143



Internal ID21393145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101364244..101365243hg38UCSC Ensembl
chr10:103124001..103125000hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15750752, nssv15745879, nssv15746119
SamplesMDQ010, MDQ025, NB09
Known GenesBTRC
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431143
Frequency
Sample Size15
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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