A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3949051



Internal ID11812821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27160512..27161159hg38UCSC Ensembl
chr1:27487003..27487650hg19UCSC Ensembl
chr1:27359590..27360237hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38648
hg19648
hg18648
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1220296
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3949051
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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