A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4313862



Internal ID11596400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107770181..107770266hg38UCSC Ensembl
chr7:107410626..107410711hg19UCSC Ensembl
chr7:107197862..107197947hg18UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3886
hg1986
hg1886
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1189776
Supporting Variants
SamplesHuRef
Known GenesSLC26A3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4313862
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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