A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17156140



Internal ID21494371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156120652..156120712hg38UCSC Ensembl
chr7:155913346..155913406hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572564
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17156140
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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