A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132772



Internal ID19249050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:58518367..58528667hg38UCSC Ensembl
OuterchrX:58544800..58555100hg19UCSC Ensembl
CytobandXp11.1
Allele length
AssemblyAllele length
hg3810301
hg1910301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987562
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132772
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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