A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607748



Internal ID16048471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88975337..89024571hg38UCSC Ensembl
Innerchr7:88604651..88653885hg19UCSC Ensembl
Innerchr7:88442587..88491821hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3849235
hg1949235
hg1849235
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155357
Samples1788485381_A
Known GenesZNF804B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607748
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