A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586375



Internal ID6973896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:71126870..71199890hg38UCSC Ensembl
chr1:71592553..71665573hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3873021
hg1973021
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv23e214
Supporting Variantsessv9964859
SamplesHG02923
Known GenesZRANB2-AS2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586375
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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