A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669125



Internal ID9588544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:21927947..22923617hg38UCSC Ensembl
Outerchr19:21927913..22923652hg38UCSC Ensembl
Innerchr19:22110749..23106419hg19UCSC Ensembl
Outerchr19:22110715..23106454hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38995740
hg19995740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv633e199
Supporting Variantsessv6378919
SamplesHG00384
Known GenesLOC100996349, LOC440518, ZNF208, ZNF257, ZNF492, ZNF676, ZNF729, ZNF98, ZNF99
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669125
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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