A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607572



Internal ID6994504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:170882366..170887972hg38UCSC Ensembl
Innerchr5:170882375..170887963hg38UCSC Ensembl
Outerchr5:170882357..170887981hg38UCSC Ensembl
chr5:170309370..170314976hg19UCSC Ensembl
Innerchr5:170309379..170314967hg19UCSC Ensembl
Outerchr5:170309361..170314985hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg385607
hg195607
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12132594
SamplesHG02944
Known GenesRANBP17
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607572
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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