A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333217



Internal ID20866393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:177955259..177962466hg38UCSC Ensembl
chr1:177924394..177931601hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg387208
hg197208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054018
Samples
Known GenesSEC16B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333217
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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