A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319246



Internal ID20852339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167923806..167924163hg38UCSC Ensembl
chr1:167893044..167893401hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053574
Samples
Known GenesMPC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319246
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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