A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607924



Internal ID6994855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3185005..3190736hg38UCSC Ensembl
Innerchr6:3185028..3190713hg38UCSC Ensembl
Outerchr6:3184982..3190759hg38UCSC Ensembl
chr6:3185239..3190970hg19UCSC Ensembl
Innerchr6:3185262..3190947hg19UCSC Ensembl
Outerchr6:3185216..3190993hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg385732
hg195732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12178841
SamplesHG03931
Known GenesLOC100507194
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607924
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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