A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657368



Internal ID9923473
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 StatusM
Merged Variants
Supporting Variantsessv6254056, essv5965461
SamplesHG01389, NA12282
Known GenesBAIAP2L1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657368
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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