A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5965461



Internal ID9261069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98364312..98364670hg38UCSC Ensembl
chr7:97993624..97993982hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38359
hg19359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2657368
Supporting Variants
SamplesNA12282
Known GenesBAIAP2L1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5965461
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