A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526672



Internal ID22396055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:75379901..75379965hg38UCSC Ensembl
chrX:74599736..74599800hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14352235, nssv14352233, nssv14352238, nssv14352239, nssv14352236, nssv14352232, nssv14352237, nssv14352234
SamplesHG00512, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesZDHHC15
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526672
Frequency
Sample Size9
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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