A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150747



Internal ID21423618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90527856..90528176hg38UCSC Ensembl
chr6:91237575..91237895hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5571500
Supporting Variants
SamplesHG00731
Known GenesMAP3K7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150747
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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