A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv957772



Internal ID16959959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:17502499..17502806hg38UCSC Ensembl
OuterchrX:17520622..17520929hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002438
SamplesBILGI_BIOE
Known GenesNHS
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv957772
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