A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976983



Internal ID19242713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:25929822..25930156hg38UCSC Ensembl
OuterchrX:25947939..25948273hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1124495
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976983
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