A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323884



Internal ID20857007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205173816..205174777hg38UCSC Ensembl
chr1:205142944..205143905hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38962
hg19962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057040
Samples
Known GenesDSTYK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323884
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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