A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606372



Internal ID16393781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20704920..20713209hg38UCSC Ensembl
Innerchr7:20744543..20752832hg19UCSC Ensembl
Innerchr7:20711068..20719357hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg388290
hg198290
hg188290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11228n54
Supporting Variantsnssv1079660
Samples
Known GenesABCB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606372
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