A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6155562



Internal ID9132965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140536750..140539046hg38UCSC Ensembl
chr7:140236550..140238846hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg382297
hg192297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673558
Supporting Variants
SamplesNA19449
Known GenesDENND2A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6155562
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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