A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990102



Internal ID12983002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65097016..65603718hg38UCSC Ensembl
Innerchr7:64557394..65068631hg19UCSC Ensembl
Innerchr7:64194829..64706066hg18UCSC Ensembl
Innerchr7:64001544..64512781hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38506703
hg19511238
hg18511238
hg17511238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752167
Supporting Variants
SamplesSPC_13
Known GenesZNF92
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6990102
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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