A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606473



Internal ID16047196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:28534721..28535285hg38UCSC Ensembl
Innerchr7:28574339..28574903hg19UCSC Ensembl
Innerchr7:28540864..28541428hg18UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg38565
hg19565
hg18565
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11246n54
Supporting Variantsnssv1081545, nssv1081523, nssv1081521, nssv1081531, nssv1081539, nssv1081549, nssv1081532, nssv1081520, nssv1081524, nssv1081525, nssv1081541, nssv1081522, nssv1081533, nssv1081534, nssv1081548, nssv1081543, nssv1081526, nssv1081537, nssv1081528, nssv1081530, nssv1081542, nssv1081544, nssv1081538, nssv1081529, nssv1081518, nssv1081519, nssv1081547, nssv1081535, nssv1081536, nssv1081527, nssv1081540, nssv1081546
Samples
Known GenesCREB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606473
Frequency
Sample Size17421
Observed Gain0
Observed Loss32
Observed Complex0
Frequencyn/a


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