A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077224



Internal ID19325071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:40096746..40105547hg38UCSC Ensembl
chrX:39955999..39964800hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg388802
hg198802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771630
SamplesKWP1
Known GenesBCOR
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077224
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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