A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv708604



Internal ID15655874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1615322..1663759hg38UCSC Ensembl
Innerchr1:1550702..1595198hg19UCSC Ensembl
Innerchr1:1540565..1585061hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3848438
hg1944497
hg1844497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545017
Supporting Variants
Samples
Known GenesCDK11B, MIB2, MMP23A, MMP23B, SLC35E2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv708604
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