A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985827



Internal ID12637413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:102824173..103074191hg38UCSC Ensembl
Innerchr7:102464620..102714638hg19UCSC Ensembl
Innerchr7:102251856..102501874hg18UCSC Ensembl
Innerchr7:102058571..102308589hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38250019
hg19250019
hg18250019
hg17250019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752138
Supporting Variants
SamplesSPC_61
Known GenesFBXL13, LRRC17
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985827
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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