A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332795



Internal ID20865970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:66627400..66628189hg38UCSC Ensembl
chr1:67093083..67093872hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38790
hg19790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062617
Samples
Known GenesSGIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332795
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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