A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1094801



Internal ID15601301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:137888441..137888916hg38UCSC Ensembl
Innerchr7:137573187..137573662hg19UCSC Ensembl
Innerchr7:137223727..137224202hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38476
hg19476
hg18476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608469
Supporting Variants
Samples
Known GenesCREB3L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1094801
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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