A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451989



Internal ID21109542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30457173..30483464hg38UCSC Ensembl
chr10:30746102..30772393hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3826292
hg1926292
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178968
Samples
Known GenesMAP3K8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451989
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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