A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690200



Internal ID18641795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39445501..40228945hg38UCSC Ensembl
Innerchr9:41475094..42373963hg19UCSC Ensembl
Innerchr9:41465094..42363959hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38783445
hg19898870
hg18898866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020579
Supporting Variants
Samples
Known GenesANKRD20A2, ANKRD20A3, KGFLP2, LOC643648, LOC653501, MGC21881, SPATA31A5, SPATA31A7, ZNF658B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690200
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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