A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333478



Internal ID20866655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:78300778..78302586hg38UCSC Ensembl
chr1:78766462..78768270hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg381809
hg191809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18063255
Samples
Known GenesMGC27382
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333478
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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