A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1102085



Internal ID5232191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3509659..3509714hg38UCSC Ensembl
chr4:3511386..3511441hg19UCSC Ensembl
chr4:3481184..3481239hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3856
hg1956
hg1856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4075328
SamplesHuRef
Known GenesLRPAP1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1102085
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