A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607972



Internal ID16048695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101096401..101167702hg38UCSC Ensembl
Innerchr7:100739682..100810983hg19UCSC Ensembl
Innerchr7:100526402..100597703hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3871302
hg1971302
hg1871302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1091883
Samples
Known GenesAP1S1, MIR4653, SERPINE1, VGF
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607972
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