A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1627506



Internal ID12790626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1145003..1146146hg38UCSC Ensembl
chr4:1138791..1139934hg19UCSC Ensembl
chr4:1128791..1129934hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381144
hg191144
hg181144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4028121
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1627506
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