A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12253932



Internal ID2255748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31139843..31176217hg38UCSC Ensembl
chr6:31107620..31143994hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3836375
hg1936375
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3608528
Supporting Variants
SamplesHG02943
Known GenesCCHCR1, POU5F1, PSORS1C1, PSORS1C3, TCF19
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12253932
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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