A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4133256



Internal ID11069109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9116185..9116185hg38UCSC Ensembl
chr1:9176244..9176244hg19UCSC Ensembl
chr1:9098831..9098831hg18UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38276
hg19276
hg18276
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1519481
Supporting Variants
SamplesHuRef
Known GenesGPR157
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4133256
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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