A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv708614



Internal ID15655884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1671348..1706566hg38UCSC Ensembl
Innerchr1:1602787..1638005hg19UCSC Ensembl
Innerchr1:1592650..1627865hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3835219
hg1935219
hg1835216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545026
Supporting Variants
Samples
Known GenesCDK11A, CDK11B, MMP23A, SLC35E2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv708614
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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