A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983535



Internal ID12629760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65384137..65447937hg38UCSC Ensembl
Innerchr7:64849050..64912850hg19UCSC Ensembl
Innerchr7:64486485..64550285hg18UCSC Ensembl
Innerchr7:64293200..64357000hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3863801
hg1963801
hg1863801
hg1763801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752165
Supporting Variants
SamplesBEC_666
Known GenesZNF92
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983535
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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