A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133764



Internal ID18927334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:52359357..52411357hg38UCSC Ensembl
OuterchrX:52102500..52154500hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3852001
hg1952001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969339
SamplesKWS2
Known GenesXAGE2, XAGE2B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133764
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer