A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3195824



Internal ID22345940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:40841715..40842159hg38UCSC Ensembl
chrX:40700968..40701412hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38445
hg19445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14350346, nssv14350347
SamplesNA19238, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3195824
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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