A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433236



Internal ID21090789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8941421..9397494hg38UCSC Ensembl
chr8:8798931..9255004hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38456074
hg19456074
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170875
Samples
Known GenesERI1, LOC157273, MIR4660, PPP1R3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433236
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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