A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153101



Internal ID19195162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:72913161..72934260hg38UCSC Ensembl
OuterchrX:72132999..72154100hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3821100
hg1921102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3998135
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153101
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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