A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984671



Internal ID12983311
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 gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752169
Supporting Variants
SamplesSPC_163
Known GenesZNF92
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984671
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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