A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615699



Internal ID6655897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157524033..157541939hg38UCSC Ensembl
chr7:157316727..157334633hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3817907
hg1917907
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13041295
SamplesHG00631
Known GenesPTPRN2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615699
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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