A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431360



Internal ID21393362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6630039..6797038hg38UCSC Ensembl
chr10:6672001..6839000hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38167000
hg19167000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15753049, nssv15750401
SamplesNB08, NB09
Known GenesLINC00706, LINC00707
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431360
Frequency
Sample Size15
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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