A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317580



Internal ID20850667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:96351201..96351800hg38UCSC Ensembl
chr1:96816757..96817356hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065324
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317580
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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