A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502859



Internal ID20876107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:94835601..94869700hg38UCSC Ensembl
chr15:95378830..95412929hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3834100
hg1934100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196018
Samples
Known GenesLOC440311
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502859
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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