A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324514



Internal ID20857642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31801357..31808674hg38UCSC Ensembl
chr1:32266958..32274275hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg387318
hg197318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060404
Samples
Known GenesSPOCD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324514
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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