A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6463004



Internal ID9753723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:74843366..74844175hg38UCSC Ensembl
chr2:75070493..75071302hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38810
hg19810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677814
Supporting Variants
SamplesNA19704
Known GenesHK2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6463004
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