A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605892



Internal ID16393301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:3301957..3385246hg38UCSC Ensembl
Innerchr7:3341589..3424878hg19UCSC Ensembl
Innerchr7:3308115..3391404hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3883290
hg1983290
hg1883290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1078498
Samples
Known GenesSDK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605892
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