A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324767



Internal ID20857895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:79311051..79311578hg38UCSC Ensembl
chr1:79776736..79777263hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38528
hg19528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064269
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324767
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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