A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3557672



Internal ID22426477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27013071..27013671hg38UCSC Ensembl
chrX:27031188..27031788hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14350731, nssv14350730, nssv14350732
SamplesNA19239, NA19240, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3557672
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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