A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151622



Internal ID19200987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:105028217..105035918hg38UCSC Ensembl
OuterchrX:104272899..104280600hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg387702
hg197702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003044
SamplesKWB1
Known GenesIL1RAPL2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151622
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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