A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316781



Internal ID20849863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:177912128..177958804hg38UCSC Ensembl
chr1:177881263..177927939hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3846677
hg1946677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054016
Samples
Known GenesSEC16B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316781
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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