A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6175389



Internal ID9854345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68001118..68002250hg38UCSC Ensembl
Outerchr10:68001081..68002300hg38UCSC Ensembl
Innerchr10:69760875..69762007hg19UCSC Ensembl
Outerchr10:69760838..69762057hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381220
hg191220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2676451
Supporting Variants
SamplesNA20521
Known GenesHERC4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6175389
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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