A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439871



Internal ID21097424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4240601..4251000hg38UCSC Ensembl
chr10:4282793..4293192hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3810400
hg1910400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980187
Samples
Known GenesLINC00702
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439871
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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