A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561907



Internal ID22430673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17437669..17437669hg38UCSC Ensembl
chr1:17764165..17764165hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14351933
SamplesHG00514
Known GenesRCC2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561907
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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