A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115257



Internal ID19268618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:27351077..27351130hg38UCSC Ensembl
OuterchrX:27369194..27369247hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3976308
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115257
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