A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001234



Internal ID18743765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16918706..16931632hg38UCSC Ensembl
Innerchr1:17245201..17258127hg19UCSC Ensembl
Innerchr1:17117788..17130714hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3812927
hg1912927
hg1812927
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv126n100
Supporting Variantsnssv3467001, nssv3464306
Samples
Known GenesCROCC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001234
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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