A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150147



Internal ID19197372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:131581925..131584726hg38UCSC Ensembl
OuterchrX:130715899..130718700hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg382802
hg192802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003447
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150147
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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