A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678817



Internal ID9598236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16488130..16636729hg38UCSC Ensembl
Outerchr1:16488096..16636764hg38UCSC Ensembl
Innerchr1:16814625..16963224hg19UCSC Ensembl
Outerchr1:16814591..16963259hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38148669
hg19148669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6308194
SamplesNA18528
Known GenesCROCCP2, CROCCP3, MIR3675, NBPF1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678817
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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