A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667810



Internal ID9587229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16510088..16662749hg38UCSC Ensembl
Outerchr1:16510054..16662784hg38UCSC Ensembl
Innerchr1:16836583..16989244hg19UCSC Ensembl
Outerchr1:16836549..16989279hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38152731
hg19152731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv21e199
Supporting Variantsessv6143838
SamplesHG00698
Known GenesCROCCP2, MIR3675, MST1P2, NBPF1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667810
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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