A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323260



Internal ID20856377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38513104..38518575hg38UCSC Ensembl
chr1:38978776..38984247hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg385472
hg195472
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061251
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323260
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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