A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330612



Internal ID20863770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:240292401..240294300hg38UCSC Ensembl
chr1:240455701..240457600hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059515
Samples
Known GenesFMN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330612
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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