A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989503



Internal ID12637411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:102824602..103072602hg38UCSC Ensembl
Innerchr7:102465049..102713049hg19UCSC Ensembl
Innerchr7:102252285..102500285hg18UCSC Ensembl
Innerchr7:102059000..102307000hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38248001
hg19248001
hg18248001
hg17248001
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)essv6989503
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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