A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325929



Internal ID20859063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:68252444..68267422hg38UCSC Ensembl
chr1:68718127..68733105hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3814979
hg1914979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062718
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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