A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17410751



Internal ID22468621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:171913931..171941738hg38UCSC Ensembl
chr4:172835082..172862889hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3827808
hg1927808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900300
Supporting Variants
Samples
Known GenesGALNTL6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17410751
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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