A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3919222



Internal ID11495963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180635828..180635920hg38UCSC Ensembl
chr5:180062828..180062920hg19UCSC Ensembl
chr5:179995434..179995526hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3893
hg1993
hg1893
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1049221
Supporting Variants
SamplesHuRef
Known GenesFLT4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3919222
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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