A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4267240



Internal ID11549778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151102694..151102791hg38UCSC Ensembl
chr6:151423830..151423927hg19UCSC Ensembl
chr6:151465523..151465620hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3898
hg1998
hg1898
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1381183
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4267240
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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