A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316237



Internal ID20849315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38440844..38442348hg38UCSC Ensembl
chr1:38906516..38908020hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381505
hg191505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061248
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316237
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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