A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3804006



Internal ID11957865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15742637..15742637hg38UCSC Ensembl
chr3:15784144..15784144hg19UCSC Ensembl
chr3:15759148..15759148hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3878
hg1978
hg1878
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1552939
Supporting Variants
SamplesHuRef
Known GenesANKRD28
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3804006
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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