A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1089437



Internal ID15595937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88922142..88942114hg38UCSC Ensembl
Innerchr7:88551456..88571428hg19UCSC Ensembl
Innerchr7:88389392..88409364hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3819973
hg1919973
hg1819973
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607747
Supporting Variants
Samples
Known GenesZNF804B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1089437
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