A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317550



Internal ID20850637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67814389..67830300hg38UCSC Ensembl
chr1:68280072..68295983hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3815912
hg1915912
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062693
Samples
Known GenesGNG12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317550
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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