A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982434



Internal ID12973734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:118099346..118146984hg38UCSC Ensembl
Innerchr7:117739400..117787038hg19UCSC Ensembl
Innerchr7:117526636..117574274hg18UCSC Ensembl
Innerchr7:117333351..117380989hg17UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3847639
hg1947639
hg1847639
hg1747639
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752146
Supporting Variants
SamplesBEC_442
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982434
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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