A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15197019



Internal ID21335815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6612831..6612991hg38UCSC Ensembl
chr6:6613064..6613224hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3940102
Supporting Variants
SamplesHG002
Known GenesLY86, LY86-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15197019
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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