A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663856



Internal ID9583275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16309278..16362574hg38UCSC Ensembl
chr7:16348903..16402199hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3853297
hg1953297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1185e199
Supporting Variantsessv6247999, essv5476491, essv5641498, essv6305613, essv5870396
SamplesHG00448, NA18635, NA18558, HG00543, HG00560
Known GenesISPD
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663856
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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