A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132237



Internal ID18915431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:19467694..19467756hg38UCSC Ensembl
OuterchrX:19485812..19485874hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3986990
SamplesKWS1
Known GenesMAP3K15
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132237
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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