A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319443



Internal ID20852537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173694309..173706374hg38UCSC Ensembl
chr1:173663448..173675513hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg3812066
hg1912066
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053138
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319443
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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