A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6515082



Internal ID9492485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:71154686..71159891hg38UCSC Ensembl
chr7:70619672..70624877hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg385206
hg195206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657279
Supporting Variants
SamplesNA19703
Known GenesWBSCR17
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6515082
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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