A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152189



Internal ID21457075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89266860..89267038hg38UCSC Ensembl
chr6:89976579..89976757hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574731
Supporting Variants
SamplesHG02587
Known GenesGABRR2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152189
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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