A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15197385



Internal ID21336181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125962255..125962315hg38UCSC Ensembl
chr6:126283401..126283461hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3929632
Supporting Variants
SamplesHG002
Known GenesHINT3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15197385
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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