A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6248931



Internal ID9226334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11928458..11934906hg38UCSC Ensembl
chr19:12039273..12045721hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg386449
hg196449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666815
Supporting Variants
SamplesNA19625
Known GenesZNF700
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6248931
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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