A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076709



Internal ID18970591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:53051717..53053718hg38UCSC Ensembl
chrX:53080899..53082900hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg382002
hg192002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770612
SamplesKWP1
Known GenesGPR173
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076709
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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