A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332460



Internal ID20865632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:217787821..217788276hg38UCSC Ensembl
chr1:217961163..217961618hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057639
Samples
Known GenesSPATA17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332460
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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