A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327897



Internal ID20861041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:170024601..170025700hg38UCSC Ensembl
chr1:169993742..169994841hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053352
Samples
Known GenesKIFAP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327897
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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