A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15941707



Internal ID5943523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76911767..77002929hg38UCSC Ensembl
chr18:74623723..74714885hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3891163
hg1991163
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643197
Supporting Variants
SamplesNA06984
Known GenesMBP, ZNF236
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15941707
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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