A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6557893



Internal ID9535296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71693862..71694125hg38UCSC Ensembl
chr10:73453619..73453882hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2658220
Supporting Variants
SamplesHG00313
Known GenesCDH23
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6557893
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer