A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17429167



Internal ID22487037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125699912..125701403hg38UCSC Ensembl
chr6:126021058..126022549hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg381492
hg191492
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5893544
Supporting Variants
Samples
Known GenesLOC643623
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17429167
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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