A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985321



Internal ID12636445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90333437..90457213hg38UCSC Ensembl
Innerchr15:90876669..91000445hg19UCSC Ensembl
Innerchr15:88677673..88801449hg18UCSC Ensembl
Innerchr15:88677673..88801449hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38123777
hg19123777
hg18123777
hg17123777
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751541
Supporting Variants
SamplesSPC_141
Known GenesGABARAPL3, IQGAP1, ZNF774
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985321
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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