A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6192583



Internal ID9169986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89324124..89324793hg38UCSC Ensembl
Innerchr7:88953438..88954107hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38670
hg19670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659894
Supporting Variants
SamplesNA19240
Known GenesZNF804B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6192583
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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