A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145405



Internal ID21488289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:34971885..34971981hg38UCSC Ensembl
chr7:35011497..35011593hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5575016
Supporting Variants
SamplesNA18939
Known GenesDPY19L1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145405
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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