A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065137



Internal ID21502509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35015743..35015743hg38UCSC Ensembl
chr1:35481344..35481344hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5617404
Supporting Variants
SamplesNA19239
Known GenesZMYM6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065137
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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