A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985509



Internal ID12626247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:61283174..63193229hg38UCSC Ensembl
Innerchr7:61265899..62653607hg19UCSC Ensembl
Innerchr7:61269841..62291042hg18UCSC Ensembl
Innerchr7:61076556..62097757hg17UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg381910056
hg191387709
hg181021202
hg171021202
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752164
Supporting Variants
SamplesBEC_361
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985509
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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