A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1533887



Internal ID12697009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35136553..35137154hg38UCSC Ensembl
chr6:35104330..35104931hg19UCSC Ensembl
chr6:35212308..35212909hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38602
hg19602
hg18602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3643941
SamplesHuRef
Known GenesTCP11
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1533887
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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