A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983533



Internal ID12629751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65263183..65447922hg38UCSC Ensembl
Innerchr7:64728078..64912835hg19UCSC Ensembl
Innerchr7:64365513..64550270hg18UCSC Ensembl
Innerchr7:64172228..64356985hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38184740
hg19184758
hg18184758
hg17184758
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)essv6983533
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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