A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976552



Internal ID19241970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:49140610..49140660hg38UCSC Ensembl
OuterchrX:48996945..48996995hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1124504
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976552
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