A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330295



Internal ID20863451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38442973..38443337hg38UCSC Ensembl
chr1:38908645..38909009hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061249
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330295
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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