A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000870



Internal ID17293822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:2499860..2502659hg38UCSC Ensembl
OuterchrX:2417901..2420700hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953397
Supporting Variants
SamplesBILGI_BIOE
Known GenesDHRSX, ZBED1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000870
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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