A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985322



Internal ID12636444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90333464..90457164hg38UCSC Ensembl
Innerchr15:90876696..91000396hg19UCSC Ensembl
Innerchr15:88677700..88801400hg18UCSC Ensembl
Innerchr15:88677700..88801400hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38123701
hg19123701
hg18123701
hg17123701
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)essv6985322
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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