A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15753049



Internal ID21389125
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 StatusS
Merged Variantsnsv4431360
Supporting Variants
SamplesNB09
Known GenesLINC00706, LINC00707
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15753049
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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