A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502869



Internal ID20876117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:33970001..34711900hg38UCSC Ensembl
chr15:34262202..35004101hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38741900
hg19741900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194850
Samples
Known GenesAVEN, CHRM5, EMC4, EMC7, GOLGA8A, GOLGA8B, KATNBL1, LPCAT4, MIR1233-1, MIR1233-2, NOP10, NUTM1, PGBD4, SLC12A6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502869
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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