A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606469



Internal ID16047192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:27181212..27207660hg38UCSC Ensembl
Innerchr7:27220831..27247279hg19UCSC Ensembl
Innerchr7:27187356..27213804hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3826449
hg1926449
hg1826449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1081515
Samples
Known GenesHOTTIP, HOXA11, HOXA11-AS, HOXA13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606469
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