A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520699



Internal ID15101306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:155545002..155699751hg38UCSC Ensembl
InnerchrX:154774663..154929412hg19UCSC Ensembl
InnerchrX:154427857..154582606hg18UCSC Ensembl
InnerchrX:154338367..154493116hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38154750
hg19154750
hg18154750
hg17154750
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv674290, nssv688059, nssv700054, nssv678628, nssv680829
Samples
Known GenesTMLHE
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520699
Frequency
Sample Size2026
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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