A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4156929



Internal ID11439467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2308487..2308623hg38UCSC Ensembl
chr11:2329717..2329853hg19UCSC Ensembl
chr11:2286293..2286429hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38137
hg19137
hg18137
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1338872
Supporting Variants
SamplesHuRef
Known GenesTSPAN32
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4156929
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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