A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6319062



Internal ID9187914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:64063500..64329639hg38UCSC Ensembl
chr7:63523878..63790017hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38266140
hg19266140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659946
Supporting Variants
SamplesHG01462
Known GenesZNF679, ZNF727, ZNF735, ZNF736
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6319062
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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