A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3643941



Internal ID12117927
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1533887
Supporting Variants
SamplesHuRef
Known GenesTCP11
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3643941
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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