A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1002962



Internal ID6715096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:130474719..130482570hg38UCSC Ensembl
Outerchr9:133350106..133357957hg19UCSC Ensembl
Outerchr9:132339927..132347778hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg387852
hg197852
hg187852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564931
SamplesHuRef
Known GenesASS1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1002962
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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