A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324703



Internal ID20857831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2597463..2607554hg38UCSC Ensembl
chr1:2528902..2538993hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3810092
hg1910092
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060562
Samples
Known GenesMMEL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324703
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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