A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065231



Internal ID21491213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40008337..40008464hg38UCSC Ensembl
chr1:40474009..40474136hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5571350
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065231
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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