A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17066018



Internal ID21486694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6107696..6107696hg38UCSC Ensembl
chr1:6167756..6167756hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5619630
Supporting Variants
SamplesNA12878
Known GenesCHD5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17066018
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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