A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074354



Internal ID19317979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:36724926..36725327hg38UCSC Ensembl
chrX:36742999..36743400hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765401
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074354
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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