A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14386002



Internal ID22300547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:95004679..95005427hg38UCSC Ensembl
chr1:95470235..95470983hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38749
hg19749
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3558192
Supporting Variants
SamplesNA19240
Known GenesALG14
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14386002
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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