A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133761



Internal ID18920800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:10015360..10015960hg38UCSC Ensembl
OuterchrX:9983400..9984000hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969335
SamplesKWS2
Known GenesWWC3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133761
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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