A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4352590



Internal ID11635128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170191574..170191764hg38UCSC Ensembl
chr6:170506798..170506988hg19UCSC Ensembl
chr6:170348723..170348913hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38191
hg19191
hg18191
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1142424
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4352590
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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