A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522873



Internal ID15450166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23923336..26134874hg38UCSC Ensembl
Innerchr20:23903973..26115510hg19UCSC Ensembl
Innerchr20:23851973..26063510hg18UCSC Ensembl
Innerchr20:23851973..26063510hg17UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg382211539
hg192211538
hg182211538
hg172211538
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698528
Samples
Known GenesABHD12, ACSS1, APMAP, CST7, ENTPD6, FAM182A, FAM182B, FLJ33581, GGTLC1, GINS1, LOC100134868, LOC284798, NANP, NCOR1P1, NINL, PYGB, SYNDIG1, VSX1, ZNF337
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522873
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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