A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17154671



Internal ID21486067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25601672..25601730hg38UCSC Ensembl
chr7:25641292..25641350hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5581742
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17154671
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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