A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1078371



Internal ID15584871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1790263..2072001hg38UCSC Ensembl
Innerchr7:1829899..2111636hg19UCSC Ensembl
Innerchr7:1796425..2078162hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38281739
hg19281738
hg18281738
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605833
Supporting Variants
Samples
Known GenesMAD1L1, MIR4655
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1078371
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