A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17063352



Internal ID21508471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:237883975..237883975hg38UCSC Ensembl
chr1:238047275..238047275hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5622436
Supporting Variants
SamplesNA20509
Known GenesLOC100130331, ZP4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17063352
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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