A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053973



Internal ID18796504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105436896..105537905hg38UCSC Ensembl
Innerchr9:108199177..108300186hg19UCSC Ensembl
Innerchr9:107238998..107340007hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38101010
hg19101010
hg18101010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697641, nssv3697642
Samples
Known GenesFSD1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053973
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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