A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061698



Internal ID21457498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15301135..15301135hg38UCSC Ensembl
chr1:15627631..15627631hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604646
Supporting Variants
SamplesHG02587
Known GenesFHAD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061698
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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