A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035127



Internal ID21944470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:2001312..2005835hg38UCSC Ensembl
chr17:1904606..1909129hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg384524
hg194524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632021
Samples
Known GenesRTN4RL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035127
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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