A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6064533



Internal ID9041936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:80102345..80115070hg38UCSC Ensembl
Outerchr15:80102308..80115120hg38UCSC Ensembl
Innerchr15:80394687..80407412hg19UCSC Ensembl
Outerchr15:80394650..80407462hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3812813
hg1912813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669126
Supporting Variants
SamplesNA18558
Known GenesZFAND6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6064533
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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