A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3805118



Internal ID11956753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6977768..6977848hg38UCSC Ensembl
chr4:6979495..6979575hg19UCSC Ensembl
chr4:7030396..7030476hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3881
hg1981
hg1881
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1699116
Supporting Variants
SamplesHuRef
Known GenesTBC1D14
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3805118
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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