A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331327



Internal ID20864490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:107193414..107193960hg38UCSC Ensembl
chr1:107736036..107736582hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38547
hg19547
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051793
Samples
Known GenesNTNG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331327
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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