A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987061



Internal ID12978265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19375920..19534140hg38UCSC Ensembl
Innerchr7:19415543..19573763hg19UCSC Ensembl
Innerchr7:19382068..19540288hg18UCSC Ensembl
Innerchr7:19188783..19347003hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38158221
hg19158221
hg18158221
hg17158221
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34500
Supporting Variants
SamplesNA07345
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987061
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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