A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073929



Internal ID19316102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:5652271..5652639hg38UCSC Ensembl
chrX:5570312..5570680hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg38369
hg19369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770614
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073929
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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