A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324441



Internal ID20857568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41081694..41082345hg38UCSC Ensembl
chr1:41547366..41548017hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38652
hg19652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060790
Samples
Known GenesSCMH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324441
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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