A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612698



Internal ID6999598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29632816..29796992hg38UCSC Ensembl
chr7:29672432..29836608hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38164177
hg19164177
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12717354
SamplesNA18552
Known GenesDPY19L2P3, LOC646762, MIR550A3, ZNRF2P2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612698
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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