A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6331737



Internal ID9309140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:61241771..61244769hg38UCSC Ensembl
Outerchr17:61241614..61244922hg38UCSC Ensembl
Innerchr17:59319132..59322130hg19UCSC Ensembl
Outerchr17:59318975..59322283hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg383309
hg193309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669962
Supporting Variants
SamplesNA18606
Known GenesBCAS3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6331737
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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