A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4247482



Internal ID11530020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:171502873..171503190hg38UCSC Ensembl
chr3:171220662..171220979hg19UCSC Ensembl
chr3:172703356..172703673hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38318
hg19318
hg18318
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1491332
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4247482
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer