A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023869



Internal ID19113086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39445501..39833345hg38UCSC Ensembl
Innerchr9:41475094..41978363hg19UCSC Ensembl
Innerchr9:41465094..41968363hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38387845
hg19503270
hg18503270
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7541n100
Supporting Variantsnssv3690165, nssv3690154, nssv3690149, nssv3690168, nssv3690152, nssv3690153, nssv3690155, nssv3690164, nssv3690159, nssv3690150, nssv3690167, nssv3690157, nssv3690160, nssv3690170, nssv3690151, nssv3690156, nssv3690158, nssv3690162, nssv3690161, nssv3690163, nssv3690169, nssv3690171, nssv3690166
Samples
Known GenesKGFLP2, 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)nsv1023869
Frequency
Sample Size11257
Observed Gain22
Observed Loss1
Observed Complex0
Frequencyn/a


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