A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138014



Internal ID337196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:112494079..112495382hg38UCSC Ensembl
chr1:113036701..113038004hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg381304
hg191304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16908910
Samples
Known GenesWNT2B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138014
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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