A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986628



Internal ID12982035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62620372..63086872hg38UCSC Ensembl
Innerchr7:62080750..62547250hg19UCSC Ensembl
Innerchr7:61718185..62184685hg18UCSC Ensembl
Innerchr7:61524900..61991400hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38466501
hg19466501
hg18466501
hg17466501
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34858
Supporting Variants
SamplesNA19116
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986628
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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