A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153295



Internal ID15855504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:26872627..26919239hg38UCSC Ensembl
Innerchr5:26872736..26919347hg19UCSC Ensembl
Innerchr5:26908493..26955104hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3846613
hg1946612
hg1846612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597679
Supporting Variants
Samples1782681091_A
Known GenesCDH9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153295
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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