A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10993617



Internal ID3859959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44660200..44705164hg38UCSC Ensembl
chr3:44701692..44746656hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3844965
hg1944965
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596037
Supporting Variants
SamplesHG03490
Known GenesZNF35
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10993617
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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