A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981611



Internal ID12972388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65263183..65778609hg38UCSC Ensembl
Innerchr7:64728078..65243596hg19UCSC Ensembl
Innerchr7:64365513..64881031hg18UCSC Ensembl
Innerchr7:64172228..64687746hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38515427
hg19515519
hg18515519
hg17515519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752171
Supporting Variants
SamplesBEC_304
Known GenesCCT6P1, INTS4L2, LOC441242, SNORA22, ZNF92
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981611
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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