A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14356880



Internal ID22196204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27107089..27108086hg38UCSC Ensembl
chr1:27433580..27434577hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38998
hg19998
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3200918
Supporting Variants
SamplesHG00731
Known GenesSLC9A1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14356880
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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