A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981958



Internal ID12974212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65263155..65447937hg38UCSC Ensembl
Innerchr7:64728050..64912850hg19UCSC Ensembl
Innerchr7:64365485..64550285hg18UCSC Ensembl
Innerchr7:64172200..64357000hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38184783
hg19184801
hg18184801
hg17184801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752168
Supporting Variants
SamplesBEC_508
Known GenesZNF92
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981958
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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