A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323064



Internal ID20856180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:69763982..69774031hg38UCSC Ensembl
chr1:70229665..70239714hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3810050
hg1910050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18063527
Samples
Known GenesLRRC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323064
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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