A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320214



Internal ID20853312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110156179..110160513hg38UCSC Ensembl
chr1:110698801..110703135hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg384335
hg194335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050845
Samples
Known GenesSLC6A17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320214
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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