A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321942



Internal ID20855051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77593001..77595700hg38UCSC Ensembl
chr1:78058686..78061385hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18063222
Samples
Known GenesZZZ3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321942
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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