A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497505



Internal ID20870712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:32139826..34373966hg38UCSC Ensembl
chr15:32432027..34666167hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg382234141
hg192234141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023547
Samples
Known GenesARHGAP11A, AVEN, CHRM5, CHRNA7, EMC4, EMC7, FMN1, GOLGA8K, GOLGA8O, GOLGA8R, GREM1, KATNBL1, LOC100131315, LOC100996255, LPCAT4, NOP10, NUTM1, PGBD4, RYR3, SCG5, SLC12A6, TMCO5B, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497505
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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