A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3811662



Internal ID11950209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9273121..9273320hg38UCSC Ensembl
chr10:9315084..9315283hg19UCSC Ensembl
chr10:9355090..9355289hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38200
hg19200
hg18200
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1265522
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3811662
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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