A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145072



Internal ID21510498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151779805..151779921hg38UCSC Ensembl
chr6:152100940..152101056hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574689
Supporting Variants
SamplesNA24385
Known GenesESR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145072
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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