A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155998



Internal ID21451790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:144892061..144892917hg38UCSC Ensembl
chr7:144589154..144590010hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38857
hg19857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574695
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155998
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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