A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605698



Internal ID16046421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:886312..889882hg38UCSC Ensembl
Innerchr7:925949..929519hg19UCSC Ensembl
Innerchr7:892475..896045hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg383571
hg193571
hg183571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1077807
Samples
Known GenesGET4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605698
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