A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4144090



Internal ID11426628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74837553..74837602hg38UCSC Ensembl
chr15:75129894..75129943hg19UCSC Ensembl
chr15:72916947..72916996hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1231258
Supporting Variants
SamplesHuRef
Known GenesULK3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4144090
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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