A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701165



Internal ID15091131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:152245497..152245827hg38UCSC Ensembl
InnerchrX:151413969..151414299hg19UCSC Ensembl
InnerchrX:151164625..151164955hg18UCSC Ensembl
InnerchrX:151084537..151084867hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38331
hg19331
hg18331
hg17331
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516934
Supporting Variants
Samples
Known GenesGABRA3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701165
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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