A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526772



Internal ID22396155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:17619310..17620044hg38UCSC Ensembl
chrX:17637430..17638164hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg38735
hg19735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14349971, nssv14349970
SamplesNA19239, NA19240
Known GenesNHS
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526772
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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