A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318073



Internal ID20851164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6334162..6336535hg38UCSC Ensembl
chr1:6394222..6396595hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg382374
hg192374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062283
Samples
Known GenesACOT7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318073
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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