A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585436



Internal ID347015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:98153509..98166781hg38UCSC Ensembl
Outerchr7:98153037..98167010hg38UCSC Ensembl
Innerchr7:97782821..97796093hg19UCSC Ensembl
Outerchr7:97782349..97796322hg19UCSC Ensembl
Innerchr7:97620757..97634029hg18UCSC Ensembl
Outerchr7:97620285..97634258hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3813974
hg1913974
hg1813974
Variant TypeOTHER complex
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275549
Supporting Variants
Samples
Known GenesLMTK2
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)essv2585436
Frequency
Sample Size1250
Observed Gain0
Observed Loss0
Observed Complex1
Frequencyn/a


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