A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14361595



Internal ID22314353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35391781..35391914hg38UCSC Ensembl
chr1:35857382..35857515hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3526202
Supporting Variants
SamplesNA19240
Known GenesZMYM4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14361595
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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