A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607752



Internal ID16395161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89887348..89896412hg38UCSC Ensembl
Innerchr7:89516662..89525726hg19UCSC Ensembl
Innerchr7:89354598..89363662hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg389065
hg199065
hg189065
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1089441, nssv1089440
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607752
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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